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Novel heterozygous sequence variant in the GLI1 underlies postaxial polydactyly.

Maryam YousafAsmat UllahZahid AzeemAyesha Isani MajeedMuhammad Iqbal MemonTahseen GhousSulman BasitWasim Ahmad
Published in: Congenital anomalies (2019)
Polydactyly is one of the most common congenital abnormal phenotype of autopod, which is characterized by extra supernumerary digit in hands/feet with or without well-developed bony structure within the digits. Preaxial polydactyly (PPD), postaxial polydactyly (PAP), and meso-axial (central) polydactyly are three different isoforms of polydactyly. Genetically, at least 10 genes have been identified causing nonsyndromic polydactyly. In the present study, we have investigated a large family segregating autosomal dominant form of nonsyndromic polydactyly. Whole exome sequencing followed by Sanger sequencing revealed a novel heterozygous missense variant (NM_005269.3; c.1064C>A; p.(Thr355Asn) in the gene GLI1 segregating with the disease phenotype within the family. This study presents first familial case of autosomal dominant form of polydactyly caused by the GLI1 variant.
Keyphrases
  • early onset
  • single cell
  • genome wide
  • intellectual disability
  • photodynamic therapy
  • autism spectrum disorder
  • gene expression
  • dna methylation
  • high resolution
  • mass spectrometry
  • genome wide identification